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Further clinical and molecular delineation of the 9q subtelo…
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
Article, Chapter
Authors: T. Kleefstra
Publication: Journal of Medical Genetics, Volume:46, Issue:9, Page(s):598-606
Published: BMJ Group, 2009
ISSN: 0022-2593
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View Full Text Source:Journal of Medical Genetics,Journal of Medical Genetics,BMJ Journals All Titles Opens in new Window
Journal:  Journal of Medical Genetics Source:BMJ Journals All Titles Opens in new Window
Collection:  BMJ Journals All Titles Opens in new Window
Coverage:
  • 1964~present; volume:1~present;issue:1~present
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